Results 211 to 220 of about 1,618,106 (339)

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas   +18 more
wiley   +1 more source

Splenic fibroblasts control marginal zone B cell movement and function via two distinct Notch2-dependent regulatory programs. [PDF]

open access: yesImmunity
Allman A   +29 more
europepmc   +1 more source

Representation of spontaneous movement by dopaminergic neurons is cell-type selective and disrupted in parkinsonism [PDF]

open access: green, 2016
Paul D. Dodson   +7 more
openalex   +1 more source

CSF Levels of NPTX2 Are Associated With Less Brain Atrophy Over Time in Cognitively Unimpaired Individuals

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez   +12 more
wiley   +1 more source

Fluorescence tracking identifies T cell movement from lymph nodes to irradiated tumors and mechanisms of T cell retention during post-radiation refilling 3240 [PDF]

open access: bronze
David J. Friedman   +11 more
openalex   +1 more source

Directed movement toward, translocation along, penetration into and exit from vascular networks by breast cancer cells in 3D

open access: gold, 2021
Deborah Wessels   +13 more
openalex   +1 more source

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